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PMID: 10748121 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Neuropilin-2 is a receptor for the vascular endothelial growth factor (VEGF) forms VEGF-145 and VEGF-165 [corrected].

The Journal of biological chemistry ·Vol. 275 ·No. 24 ·2000-06-16 ·Pages 18040-5

Gluzman-Poltorak Z, Cohen T, Herzog Y, Neufeld G

Abstract

Neuropilin-1 (np-1) and neuropilin-2 (np-2) are receptors for axon guidance factors belonging to the class 3 semaphorins. np-1 also binds to the 165-amino acid heparin-binding form of VEGF (VEGF(165)) but not to the shorter VEGF(121) form, which lacks a heparin binding ability. We report that human umbilical vein-derived endothelial cells express the a17 and a22 splice forms of the np-2 receptor. Both np-2 forms bind VEGF(165) with high affinity in the presence of heparin (K(D) 1.3 x 10(-10) m) but not VEGF(121). np-2 also binds the heparin-binding form of placenta growth factor. These binding characteristics resemble those of np-1. VEGF(145) is a secreted heparin binding VEGF form that contains the peptide encoded by exon 6 of VEGF but not the peptide encoded by exon 7, which is present in VEGF(165). VEGF(145) binds to np-2 with high affinity (K(D) 7 x 10(-10) m). Surprisingly, VEGF(145) did not bind to np-1. Indeed, VEGF(145) does not bind to MDA-MB-231 breast cancer cells, which predominantly express np-1. By contrast, VEGF(145) binds to human umbilical vein-derived endothelial cells, which express both np-1 and np-2. The binding of VEGF(165) to porcine aortic endothelial cells expressing recombinant np-2 did not affect the proliferation or migration of the cells. Nevertheless, it is possible that VEGF-induced np-2-mediated signaling will take place only in the presence of other VEGF receptors such as VEGF receptor-1 or VEGF receptor-2.

MeSH Terms
Animals Baculoviridae Breast Neoplasms/metabolism Cells, Cultured Electrophoresis, Polyacrylamide Gel Endothelial Growth Factors/metabolism Endothelium/metabolism Female Growth Substances/metabolism Humans Lymphokines/metabolism Nerve Tissue Proteins/metabolism Neuropilin-1 Placenta Placenta Growth Factor Pregnancy Proteins/metabolism Protein Binding Protein Isoforms/metabolism Receptors, Cell Surface/metabolism Spodoptera Structure-Activity Relationship Tumor Cells, Cultured Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors
Chemicals
Endothelial Growth Factors Growth Substances Lymphokines Nerve Tissue Proteins PGF protein, human Pregnancy Proteins Protein Isoforms Receptors, Cell Surface VEGFA protein, human Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors Placenta Growth Factor Neuropilin-1
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gluzman-Poltorak Z
Department of Biology, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Cohen T
Herzog Y
Neufeld G
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-06-16
Pages
18040-5
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Corrections
ErratumIn
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